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Humelock II Cementless Shoulder System

FDA UDI

Class II (US FDA UDI)

by Fx Solutions

Identity

Trade Name
Humelock II Cementless Shoulder System FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
Humelock II Cementless Shoulder System, CORTICAL SCREW TA6V Ø4.5mm L.36mm FDA UDI
Model / Reference
LENGTH 36 mm FDA UDI
Description
Humelock II Cementless Shoulder System, CORTICAL SCREW TA6V Ø4.5mm L.36mm FDA UDI

Identifiers

Catalog Number
107-4536 FDA UDI
Primary DI / UDI-DI
03701037302019 FDA UDI
510(k) Number
K130759 FDA UDI
FDA Product Code
HSD FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3690 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 36 Millimeter FDA UDI

Category: Orthopaedic bone screw (non-sliding)

Humelock II Cementless Shoulder System by Fx Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fx Solutions

Sources (1)

  • FDA UDI 39c22445-4719-4415-b4c0-dcfa182312a0 38 fields · synced May 31, 2026